EP1788023A1 - Multimodal polypropylene polymer composition - Google Patents
Multimodal polypropylene polymer composition Download PDFInfo
- Publication number
- EP1788023A1 EP1788023A1 EP05257141A EP05257141A EP1788023A1 EP 1788023 A1 EP1788023 A1 EP 1788023A1 EP 05257141 A EP05257141 A EP 05257141A EP 05257141 A EP05257141 A EP 05257141A EP 1788023 A1 EP1788023 A1 EP 1788023A1
- Authority
- EP
- European Patent Office
- Prior art keywords
- propylene
- polymer
- ethylene
- composition
- polymer composition
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Withdrawn
Links
Images
Classifications
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L23/00—Compositions of homopolymers or copolymers of unsaturated aliphatic hydrocarbons having only one carbon-to-carbon double bond; Compositions of derivatives of such polymers
- C08L23/02—Compositions of homopolymers or copolymers of unsaturated aliphatic hydrocarbons having only one carbon-to-carbon double bond; Compositions of derivatives of such polymers not modified by chemical after-treatment
- C08L23/10—Homopolymers or copolymers of propene
- C08L23/14—Copolymers of propene
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08J—WORKING-UP; GENERAL PROCESSES OF COMPOUNDING; AFTER-TREATMENT NOT COVERED BY SUBCLASSES C08B, C08C, C08F, C08G or C08H
- C08J5/00—Manufacture of articles or shaped materials containing macromolecular substances
- C08J5/18—Manufacture of films or sheets
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L23/00—Compositions of homopolymers or copolymers of unsaturated aliphatic hydrocarbons having only one carbon-to-carbon double bond; Compositions of derivatives of such polymers
- C08L23/02—Compositions of homopolymers or copolymers of unsaturated aliphatic hydrocarbons having only one carbon-to-carbon double bond; Compositions of derivatives of such polymers not modified by chemical after-treatment
- C08L23/10—Homopolymers or copolymers of propene
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L23/00—Compositions of homopolymers or copolymers of unsaturated aliphatic hydrocarbons having only one carbon-to-carbon double bond; Compositions of derivatives of such polymers
- C08L23/02—Compositions of homopolymers or copolymers of unsaturated aliphatic hydrocarbons having only one carbon-to-carbon double bond; Compositions of derivatives of such polymers not modified by chemical after-treatment
- C08L23/10—Homopolymers or copolymers of propene
- C08L23/14—Copolymers of propene
- C08L23/142—Copolymers of propene at least partially crystalline copolymers of propene with other olefins
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08F—MACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVING CARBON-TO-CARBON UNSATURATED BONDS
- C08F210/00—Copolymers of unsaturated aliphatic hydrocarbons having only one carbon-to-carbon double bond
- C08F210/04—Monomers containing three or four carbon atoms
- C08F210/06—Propene
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08J—WORKING-UP; GENERAL PROCESSES OF COMPOUNDING; AFTER-TREATMENT NOT COVERED BY SUBCLASSES C08B, C08C, C08F, C08G or C08H
- C08J2323/00—Characterised by the use of homopolymers or copolymers of unsaturated aliphatic hydrocarbons having only one carbon-to-carbon double bond; Derivatives of such polymers
- C08J2323/02—Characterised by the use of homopolymers or copolymers of unsaturated aliphatic hydrocarbons having only one carbon-to-carbon double bond; Derivatives of such polymers not modified by chemical after treatment
- C08J2323/10—Homopolymers or copolymers of propene
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L2205/00—Polymer mixtures characterised by other features
- C08L2205/02—Polymer mixtures characterised by other features containing two or more polymers of the same C08L -group
Definitions
- This invention relates to a polypropylene based copolymer composition that is suitable for making biaxially oriented films or articles, particularly biaxially-oriented containers, using injection stretch blow moulding (ISBM) processes.
- the invention concerns a polymer blend comprising a random copolymer of propylene and ethylene and a second polymer comprising either a second random copolymer of propylene and ethylene or a propylene homopolymer.
- the ISBM process involves producing a preform by injection moulding followed by stretching and blowing the preform in order to induce biaxial orientation in the solid phase.
- ISBM processes are used to make containers such as bottles and jars having very good optical properties.
- Poly(ethylene terephthalate) (PET) is the most commonly used polymer for ISBM applications because PET has good processing behaviour and produces high quality bottles having good optical and barrier properties.
- PET is however a relatively expensive polymer and cannot function at higher temperatures due to poor heat resistance. The skilled man is thus looking for alternatives to PET for ISBM applications.
- Polypropylene is considerably cheaper than PET and demonstrates better heat resistance than PET. In some applications, particularly when high temperature resistance is required, it would therefore be advantageous to use polypropylene instead of PET in ISBM processes.
- polypropylene has a narrow processing window when used in ISBM processes, i.e. polypropylene can be stretched or blown only over a narrow temperature range.
- polypropylene typically possess a 5°C processing window whereas PET can be processed over 15°C. This narrow range is not favourable industrially since temperature control becomes a large issue.
- the present inventors have therefore been addressing the problem of broadening the processing window of polypropylene whilst trying to maintain satisfactory optical and mechanical properties required of ISBM containers.
- polypropylene homopolymers may improve stiffness, they are translucent leading to poor optical properties.
- random copolymers of propylene and ethylene have good optical properties but are not as stiff as polypropylene homopolymers.
- EP-A-0339804 discloses blends of a propylene/olefin random copolymer and substantially isotactic homopolypropylene. The polymers are biaxially stretched in order to produce a bi-oriented film. The olefin is preferably ethylene and is present in the final polymer in an amount of up to about 5 mol %.
- the polymer blends of EP-A-0339804 have a melt flow rate (MFR) of around 2.1 to 3.2 g/10 min.
- the present inventors have surprisingly found that a blend of polypropylene polymers having an overall MFR of 6 to 30 (measured according to ISO 1133 at 230°C and a load of 2.16 kg) possess not only excellent mechanical properties and optical properties but also a broadened processing window.
- the blend comprises a random copolymer of propylene and ethylene/other comonomer and a second polymer selected from polypropylene homopolymer or a second (different) random copolymer of propylene and ethylene/comonomer.
- This blend has been found to possess very low haze and a processing window of similar breadth to that of PET and offers therefore an ideal replacement for PET in ISBM applications.
- the high MFR values allows higher throughputs on film lines or in moulding processes and, in particular in injection moulding applications, reduces the power needed to effect the stretching in the ISBM process.
- the invention provides a multimodal polymer composition comprising:
- the invention provides a process for the preparation of an article, the process comprising injection moulding a polymer composition as hereinbefore defined to prepare a preform and subsequently biaxially stretching and blowing the preform at a temperature below the melting point of the polymer.
- the invention provides a process for the preparation of a polymer composition as hereinbefore described the comprising in a first slurry stage polymerising propylene and optionally ethylene and/or C 4-10 alpha olefin in the presence of a Ziegler Natta catalyst so as to form
- the invention provides the use of a polymer composition as hereinbefore described for the manufacture of a film or article by blow moulding, film blowing, film casting or ISBM.
- the invention provides film or article having biaxial molecular orientation comprising a polymer composition as hereinbefore described.
- the polymer composition of the present invention preferably comprises 10 to 90 wt % of polymer A, preferably 30 to 70 wt %, more preferably 40 to 60 wt % and most preferably 45 to 55 wt %.
- the composition preferably comprises 10 to 90 wt % of polymer B, preferably 30 to 70 wt %, more preferably 40 to 60 wt % and most preferably 45 to 55 wt %.
- Polymer A preferably comprises up to 2.5 wt % comonomer, more preferably up to 2 wt % comonomer. Where polymer A is copolymeric, the comonomer is preferably ethylene. Most preferably however, polymer A is a polypropylene homopolymer.
- the MFR of polymer A may vary depending on whether it is a homopolymer or a copolymer.
- Homopolymers may have an MFR in the range 2 to 20 g/10 min, e.g. 5 to 15 g/10 min.
- Copolymers may have lower MFR's in general with values ranging from 0.5 to 10 g/10 min, e.g. 1 to 5 g/10 min.
- the density of this component may be around 890 to 920 kg/m 3 , e.g. 900 to 910 kg/m 3 .
- the isotacticity of component (A) when it is a homopolymer may be as high as 98% although will preferably be at least 85 %, e.g. in the range 90 to 95 %.
- Polymer B generally has an MFR of similar value to that of polymer A, e.g. within 5 g/10 min thereof, preferably within 3 g/10 min thereof.
- the comonomer content of polymer B may be in the range 0.5 to 10 wt %, preferably 2.5 to 7 wt %, and most preferably 3.5 to 6 wt %.
- a preferred comonomer is ethylene. Where both components A and B are copolymeric, it is preferred if component B has a higher comonomer content. It will be appreciated that in certain circumstances it will be impossible to measure the properties of either polymer A or polymer B directly e.g. when a component is made second in a multistage process. The person skilled in the art will be able to work out the properties of each component from measurements taken on the first formed component and the overall properties of the polymer composition.
- the total comonomer content of the polymer composition is preferably 1 to 5 wt %, more preferably at least 2.5 wt%, e.g. 2.5 to 4 wt %, and most preferably 3 to 4.0 wt %, e.g. 3 to 3.5 wt%.
- the polymer of the present invention has a melt flow rate of at least 6 g/10min, e.g. 6 to 50 g/10 min, preferably 7 to 40 g/10min when measured according to ISO 1133 at 230 °C and a load of 2.16 kg.
- the melt flow rate is 6 to 35 g/10 min, most preferably 8 to 30 g/10 min.
- the xylene soluble fraction of the polymer composition can range from 0.1 to 20 %, preferably 5 to 15 wt%.
- the melting point of the polymer composition may range from 150 to 180°C, preferably around 160 to 170°C.
- the polymer composition should also be partially crystalline, e.g. having a crystallinity of the order of 20 to 50 %, e.g. 25 to 40%.
- the propylene composition of the invention may also have an average of at least 50, e.g. at least 60, preferably at least 70 chain disruptor units per 1000 propylene repeating units.
- the disruptor units are formed racemic propylene diads and by comonomer incorporated into the propylene chain. The remainder of the propylene will thus be formed by meso diads.
- the number of racemic disruptors per 1000 repeat units is defined by the number of racemic sequences disrupting the continuous meso sequences.
- the total racemic diad [r] and the racemic tetrad [rrr] concentrations are required to determine the total number of times an isotactic chain is punctuated by either a pair of racemic diads or sequences involving racemic diads.
- the typical punctuating sequences in an isotactic homopolypropylene are:
- the processing window (measured as described fully below) should be at least 10°C, preferably at least 12°C, more preferably at least 15°C, especially at least 20°C.
- the polymer of the invention is multimodal, preferably bimodal, i.e. its molecular weight profile does not comprise a single peak but instead comprises the combination of two or more peaks (which may or may not be distinguishable) centred about different average molecular weights as a result of the fact that the polymer comprises two or more separately produced components. It is believed that the multimodal nature of the claimed composition allows improvements in processing properties. It is preferred therefore if there is multimodality in the ethylene content of the components.
- both components of the polymer are copolymeric, it is required that the polymers are different to ensure that the polymer composition is multimodal.
- the nature of the comonomer used in each component will be different or the amount of comonomer used in each component will be different, e.g. at least differing by 1 wt%, e.g. at least 2 wt%, preferably at least 3 wt%.
- the molecular weight distribution of the composition is an important factor.
- Such multimodal polymers may be prepared by simple blending, by two or more stage polymerisation or by the use of two or more different polymerisation catalysts in a one stage polymerisation. Preferably however they are produced in a two-stage polymerisation using the same catalyst, e.g. a metallocene catalyst or preferably a Ziegler-Natta catalyst, in particular a slurry polymerisation in a loop reactor followed by a gas phase polymerisation in a gas phase reactor. Conventional cocatalysts, supports/carriers, electron donors etc. can be used.
- a loop reactor - gas phase reactor system is marketed by Borealis A/S, Denmark as a BORSTAR reactor system.
- the polymer of the invention is thus preferably formed in a two stage process comprising a first slurry loop polymerisation followed by gas phase polymerisation in the presence of a Ziegler-Natta catalyst.
- the reaction temperature will generally be in the range 60 to 110°C (e.g. 85-110°C)
- the reactor pressure will generally be in the range 5 to 80 bar (e.g. 50-65 bar)
- the residence time will generally be in the range 0.3 to 5 hours (e.g. 0.5 to 2 hours).
- the diluent used will generally be an aliphatic hydrocarbon having a boiling point in the range -70 to +100°C. In such reactors, polymerisation may if desired be effected under supercritical conditions.
- the reaction temperature used will generally be in the range 60 to 115°C (e.g. 70 to 110°C)
- the reactor pressure will generally be in the range 10 to 25 bar
- the residence time will generally be 1 to 8 hours.
- the gas used will commonly be a non-reactive gas such as nitrogen or low boiling point hydrocarbons such as propane together with the monomer (i.e. propylene and ethylene when required).
- component A of the polymer of the invention is produced in a continuously operating loop reactor where propylene (and comonomer when required) are polymerised in the presence of a polymerisation catalyst as stated above and a chain transfer agent such as hydrogen.
- the diluent is typically an inert aliphatic hydrocarbon, preferably isobutane or propane.
- Component B can then be formed in a gas phase reactor using the same catalyst.
- Prepolymerisation can be employed as is well known in the art.
- Ziegler-Natta catalysts are preferred. The nature of the Ziegler-Natta catalyst is described in numerous prior publications, e.g. US 5234879 .
- the polymers of the invention can be made by blending two random copolymers of propylene or by blending one random copolymer with a polypropylene homopolymer in a conventional blending apparatus.
- Random copolymers of propylene and propylene homopolymers of use in this invention are commercially available from various suppliers, e.g. Borealis A/S.
- the polymer composition of the present invention has a higher MFR than those known in the art.
- Propylene polymers and copolymers can be modified by chemical cracking of the polymer chains often called visbreaking. Visbreaking is carried out in an extruder before moulding operations using organic peroxides with relatively high molar mass in a controlled manner. Statistically higher molar mass chains are cleaved more frequently than are lower molar mass molecules, resulting in an overall decrease in the average molar mass and an increase in MFR.
- the amount of peroxide fed into the extruder is controlled to reach the desired molar mass and MFR, and depends on the MFR of the reactor product.
- the formed polypropylene is often termed controlled rheology polypropylene and shows a number of advantages regarding processability, mechanics and optics.
- Suitable amounts of peroxide are around 0.01 to 0.1 1 wt%.
- the polymer composition of the invention can include minor amounts of standard polymer additives such as polymer processing agent, nucleating agents, anti-oxidants, UV stabilisers etc.
- the polymers of the invention are suitable for use in the manufacture of films or articles by injection moulding, film blowing, film casting or by blow moulding.
- the polymers of the invention are suitable for the production of articles having biaxial molecular orientation manufactured using ISBM processes.
- Preferred articles are bottles, e.g. of 100 ml to 10 L in volume, e.g. 300 ml or 500 ml.
- Biaxial orientation improves the physical and optical properties of the polymer, as well as improving the barrier properties.
- Biaxial molecular orientation is achieved by stretching the polymer at temperatures below the polymer melting point. In ISBM processes biaxial stretching is achieved in the stretch blow moulding step.
- the stretching temperatures used are between 110°C and 160 °C, e.g. 130°C. Stretching speeds may range from 20 to 40 m/min in both TD and MD.
- Control of the temperature of the polymer during the biaxial stretching step is critical. If the temperature is too high the stretched polymer will include areas of melted polymer, which reduces the molecular orientation, and will show variation in sample thickness. If the temperature is too low it will not be possible to biaxially stretch the polymer without the polymer failing.
- the processing window for any given polymer is the temperature range over which the polymer can in practice be biaxially stretched.
- the processing window for biaxial stretching is defined as the difference between the Max. temp and Min. temp wherein:
- the polymer compositions of the invention exhibit excellent mechanical and optical properties. Haze values of less than 10%, preferably less than 8% are achievable. It is envisaged that the polymer composition of the invention, when biaxially stretched results in a surface of more perfect molecular orientation leading to improved clarity.
- Tensile modulus values of greater than 600 MPa, e.g. greater than 650 MPa, preferably greater than 700 MPa are also achievable with the polymer composition of the invention. In general, higher ethylene contents are associated with lower tensile modulus values.
- Charpy (23°C), notched values are of the order of 5 to 10 kJ/m 2 .
- Figure 1 is a plot of the drawing force in the transverse direction as a function of the drawing temperature for Example 1 and Comparative Example 1.
- Figure 2 show the processing window for each of Examples 1 to 6, and Comparative Examples 1 and 2.
- Figure 3 shows Haze as a function of drawing temperature for samples 2, 5 and 6 and comparative Example 1.
- Sample 1 is a 60/40 wt.% blend of polymers (iv) and (v) respectively, prepared by physical mixing of polymers (iv) and (v) for 3 minutes, followed by compounding in a Prism 24mm double screw extruder at the conditions: Set temperature 230°C (melt temperature 250°C) N2 pressure: 1.5 bars Speed: 300 rpm Die Pressure: 80 bars
- Sample 2 is a 65/35 wt.% blend of polymers (i) and (ii) respectively, prepared by physical mixing of polymers (i) and (ii) for 3 minutes, followed by compounding in a Prism 24mm double screw extruder at the conditions for sample 1.
- Samples 3 to 5 are formed by blending polymer (i) and (iii) in a 60:40 weight ratio, prepared by physical mixing of polymers (i) and (iii) for 3 minutes, followed by compounding in a Prism 24mm double screw extruder at the conditions for sample 1.
- Sample 6 is formed by blending polymer (i) and (iii) in a 50:50 weight ratio, prepared by physical mixing of polymers (i) and (iii) for 3 minutes, followed by compounding in a Prism 24mm double screw extruder at the conditions for sample 1.
- a continuous multistage process was used to produce a polymer blend.
- the process comprised a prepolymerisation step, a loop reactor polymerisation and a fluidized bed gas phase reactor polymerisation.
- the catalyst used was highly active, stereospecific transesterified MgCl 2 -supported Ziegler-Natta catalyst prepared according to US 5,234,879 at a titanization temperature of 135 °C.
- the catalyst was contacted with a cocatalyst (triethylaluminium, TEAL), and an external donor (donor D, dicyclopentyl dimethoxysilane) with the Al/Ti ratio of 200 and an Al/D ratio of 5, to yield the catalyst system.
- TEAL triethylaluminium
- donor D dicyclopentyl dimethoxysilane
- the catalyst system and propylene were fed into the prepolymerisation reactor which was operated at 30°C.
- the prepolymerised catalyst was used in the subsequent polymerisation reactors.
- Propylene and hydrogen and the prepolymerised catalyst were fed into the loop reactor which was operated as a bulk reactor at the temperatures as indicated in Table 1 and a pressure of 55 bar.
- the polymer slurry stream was fed from the loop reactor into the gas phase reactor which was operated at the temperatures as indicated in Table 1 and a pressure of 20 bar.
- Propylene, ethylene and hydrogen were fed into the gas phase reactor to control the desired properties of the final polymer.
- Table 1 Unit Example 7 Al/D mol/mol 5 Al/Ti mol/mol 200 Production split (loop:GPR) mol 42:58 Loop Temperature °C 85 MFR g/10 min 20.9 GPR Temperature °C 85 Final Product Ethylene wt.% 3.7 MFR 2 g/10 min 19 XS wt.% 10.3 T m °C 165 Crystallinity % 35 SHI (0/50) Pa 5.8
- Comparative Example 1 is formed from polymer (vi) only and comparative Example 2 formed from polymer (vii) only.
- the plaques were heated in a heating chamber by IR radiation, for a defined period of time 120s before drawing.
- the maximum stretch speed of 35m/min was used.
- the stretch ratio of 3.5 x 3.5 was selected in order to achieve a thickness reduction from 2 mm to 0.2mm (same as in ISBM process).
- force elongation curves were recorded in the machine direction and in the transverse direction.
- Figure 2 and Table 3 show the processing window for each of Examples 1 to 6, and Comparative Examples 1 and 2.
- the processing window is represented by the shaded area.
- the number shown for each Example is the processing window in °C.
- Table 3 Polymer Processing window °C Sample 1 20 Sample 2 17 Sample 3 17 Sample 4 19 Sample 5 17 Sample 6 18 Comp 1 9 Comp 2 12
- the polymers of the present invention provide a significantly broader processing window for ISBM processes than the polymers of the Comparative Examples.
Landscapes
- Chemical & Material Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Medicinal Chemistry (AREA)
- Polymers & Plastics (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- Manufacturing & Machinery (AREA)
- Engineering & Computer Science (AREA)
- Crystallography & Structural Chemistry (AREA)
- Materials Engineering (AREA)
- Compositions Of Macromolecular Compounds (AREA)
- Addition Polymer Or Copolymer, Post-Treatments, Or Chemical Modifications (AREA)
- Manufacture Of Macromolecular Shaped Articles (AREA)
Abstract
A multimodal polymer composition comprising:
(A) a polypropylene homopolymer or a propylene random copolymer comprising propylene and up to 5 weight % of comonomer selected from ethylene and/or C4-10 alpha olefin; and
(B) a random copolymer of propylene and comonomer selected from ethylene and/or C4-10 alpha olefin;
wherein the total comonomer content of the polymer composition is at least 0.5 wt% and the melt flow rate of the polymer blend is at least 6 g/10 min when measured according to ISO 1133 at 230°C and a load of 2.16 kg.
(A) a polypropylene homopolymer or a propylene random copolymer comprising propylene and up to 5 weight % of comonomer selected from ethylene and/or C4-10 alpha olefin; and
(B) a random copolymer of propylene and comonomer selected from ethylene and/or C4-10 alpha olefin;
wherein the total comonomer content of the polymer composition is at least 0.5 wt% and the melt flow rate of the polymer blend is at least 6 g/10 min when measured according to ISO 1133 at 230°C and a load of 2.16 kg.
Description
- This invention relates to a polypropylene based copolymer composition that is suitable for making biaxially oriented films or articles, particularly biaxially-oriented containers, using injection stretch blow moulding (ISBM) processes. In particular, the invention concerns a polymer blend comprising a random copolymer of propylene and ethylene and a second polymer comprising either a second random copolymer of propylene and ethylene or a propylene homopolymer.
- The ISBM process involves producing a preform by injection moulding followed by stretching and blowing the preform in order to induce biaxial orientation in the solid phase. ISBM processes are used to make containers such as bottles and jars having very good optical properties. Poly(ethylene terephthalate) (PET) is the most commonly used polymer for ISBM applications because PET has good processing behaviour and produces high quality bottles having good optical and barrier properties.
- PET is however a relatively expensive polymer and cannot function at higher temperatures due to poor heat resistance. The skilled man is thus looking for alternatives to PET for ISBM applications.
- Polypropylene is considerably cheaper than PET and demonstrates better heat resistance than PET. In some applications, particularly when high temperature resistance is required, it would therefore be advantageous to use polypropylene instead of PET in ISBM processes. However, polypropylene has a narrow processing window when used in ISBM processes, i.e. polypropylene can be stretched or blown only over a narrow temperature range. Thus, polypropylene typically possess a 5°C processing window whereas PET can be processed over 15°C. This narrow range is not favourable industrially since temperature control becomes a large issue.
- The present inventors have therefore been addressing the problem of broadening the processing window of polypropylene whilst trying to maintain satisfactory optical and mechanical properties required of ISBM containers. In this regard, whilst polypropylene homopolymers may improve stiffness, they are translucent leading to poor optical properties. On the other hand random copolymers of propylene and ethylene have good optical properties but are not as stiff as polypropylene homopolymers. There is therefore a need for a polymer composition that has the heat resistance properties of polypropylene combined with the good optical and barrier properties of PET, which can be processed over a wide temperature range in ISBM processes.
- It is known to blend polypropylene homopolymer with a random copolymer of propylene and ethylene in order to provide a polymer having good mechanical and optical properties.
EP-A-0339804 discloses blends of a propylene/olefin random copolymer and substantially isotactic homopolypropylene. The polymers are biaxially stretched in order to produce a bi-oriented film. The olefin is preferably ethylene and is present in the final polymer in an amount of up to about 5 mol %. The polymer blends ofEP-A-0339804 have a melt flow rate (MFR) of around 2.1 to 3.2 g/10 min. - The present inventors have surprisingly found that a blend of polypropylene polymers having an overall MFR of 6 to 30 (measured according to ISO 1133 at 230°C and a load of 2.16 kg) possess not only excellent mechanical properties and optical properties but also a broadened processing window. The blend comprises a random copolymer of propylene and ethylene/other comonomer and a second polymer selected from polypropylene homopolymer or a second (different) random copolymer of propylene and ethylene/comonomer. This blend has been found to possess very low haze and a processing window of similar breadth to that of PET and offers therefore an ideal replacement for PET in ISBM applications.
- Moreover, the high MFR values allows higher throughputs on film lines or in moulding processes and, in particular in injection moulding applications, reduces the power needed to effect the stretching in the ISBM process.
- Thus, viewed from one aspect, the invention provides a multimodal polymer composition comprising:
- (A) a polypropylene homopolymer or a propylene random copolymer comprising propylene and up to 5 weight % of comonomer selected from ethylene and/or C4-10 alpha olefin; and
- (B) a random copolymer of propylene and comonomer selected from ethylene and/or C4-10 alpha olefin;
- Viewed from another aspect the invention provides a process for the preparation of an article, the process comprising injection moulding a polymer composition as hereinbefore defined to prepare a preform and subsequently biaxially stretching and blowing the preform at a temperature below the melting point of the polymer.
- Viewed from another aspect the invention provides a process for the preparation of a polymer composition as hereinbefore described the comprising in a first slurry stage polymerising propylene and optionally ethylene and/or C4-10 alpha olefin in the presence of a Ziegler Natta catalyst so as to form
- (A) a polypropylene homopolymer or a propylene random copolymer comprising propylene and up to 5 weight % of comonomer selected from ethylene and/or C4-10 alpha olefin;
transferring the product mixture to a gas phase reactor and subsequently polymerising propylene and ethylene and/or C4-10 alpha olefin so as to form - (B) a random copolymer of propylene and comonomer selected from ethylene or C4-10 alpha olefin;
wherein the total comonomer content of the polymer composition is at least 0.5 wt%, e.g. 0.5 to 6 weight % and the melt flow rate of the polymer blend is at least 6 g/10 min when measured according to ISO 1133 at 230°C and a load of 2.16 kg. - Viewed from another aspect the invention provides the use of a polymer composition as hereinbefore described for the manufacture of a film or article by blow moulding, film blowing, film casting or ISBM.
- Viewed from another aspect the invention provides film or article having biaxial molecular orientation comprising a polymer composition as hereinbefore described.
- The polymer composition of the present invention preferably comprises 10 to 90 wt % of polymer A, preferably 30 to 70 wt %, more preferably 40 to 60 wt % and most preferably 45 to 55 wt %. Conversely therefore, the composition preferably comprises 10 to 90 wt % of polymer B, preferably 30 to 70 wt %, more preferably 40 to 60 wt % and most preferably 45 to 55 wt %.
- Polymer A preferably comprises up to 2.5 wt % comonomer, more preferably up to 2 wt % comonomer. Where polymer A is copolymeric, the comonomer is preferably ethylene. Most preferably however, polymer A is a polypropylene homopolymer.
- The MFR of polymer A may vary depending on whether it is a homopolymer or a copolymer. Homopolymers may have an MFR in the
range 2 to 20 g/10 min, e.g. 5 to 15 g/10 min. Copolymers may have lower MFR's in general with values ranging from 0.5 to 10 g/10 min, e.g. 1 to 5 g/10 min. - The density of this component may be around 890 to 920 kg/m3, e.g. 900 to 910 kg/m3.
- The isotacticity of component (A) when it is a homopolymer may be as high as 98% although will preferably be at least 85 %, e.g. in the range 90 to 95 %.
- Polymer B generally has an MFR of similar value to that of polymer A, e.g. within 5 g/10 min thereof, preferably within 3 g/10 min thereof. The comonomer content of polymer B may be in the range 0.5 to 10 wt %, preferably 2.5 to 7 wt %, and most preferably 3.5 to 6 wt %. A preferred comonomer is ethylene. Where both components A and B are copolymeric, it is preferred if component B has a higher comonomer content. It will be appreciated that in certain circumstances it will be impossible to measure the properties of either polymer A or polymer B directly e.g. when a component is made second in a multistage process. The person skilled in the art will be able to work out the properties of each component from measurements taken on the first formed component and the overall properties of the polymer composition.
- The total comonomer content of the polymer composition is preferably 1 to 5 wt %, more preferably at least 2.5 wt%, e.g. 2.5 to 4 wt %, and most preferably 3 to 4.0 wt %, e.g. 3 to 3.5 wt%.
- The polymer of the present invention has a melt flow rate of at least 6 g/10min, e.g. 6 to 50 g/10 min, preferably 7 to 40 g/10min when measured according to ISO 1133 at 230 °C and a load of 2.16 kg. Preferably the melt flow rate is 6 to 35 g/10 min, most preferably 8 to 30 g/10 min.
- The xylene soluble fraction of the polymer composition can range from 0.1 to 20 %, preferably 5 to 15 wt%. The melting point of the polymer composition may range from 150 to 180°C, preferably around 160 to 170°C. The polymer composition should also be partially crystalline, e.g. having a crystallinity of the order of 20 to 50 %, e.g. 25 to 40%.
- The propylene composition of the invention may also have an average of at least 50, e.g. at least 60, preferably at least 70 chain disruptor units per 1000 propylene repeating units. The disruptor units are formed racemic propylene diads and by comonomer incorporated into the propylene chain. The remainder of the propylene will thus be formed by meso diads.
- For the purposes of the present invention, the number of racemic disruptors per 1000 repeat units is defined by the number of racemic sequences disrupting the continuous meso sequences. Quantitatively, the total racemic diad [r] and the racemic tetrad [rrr] concentrations are required to determine the total number of times an isotactic chain is punctuated by either a pair of racemic diads or sequences involving racemic diads. The typical punctuating sequences in an isotactic homopolypropylene are:
- m m m m m m m r r m m m m m m m m m -
- m m m m m m r (r)n r m m m m m m -
- m m m m m m r(m)n r m m m m m m -
-
- The processing window (measured as described fully below) should be at least 10°C, preferably at least 12°C, more preferably at least 15°C, especially at least 20°C.
- The polymer of the invention is multimodal, preferably bimodal, i.e. its molecular weight profile does not comprise a single peak but instead comprises the combination of two or more peaks (which may or may not be distinguishable) centred about different average molecular weights as a result of the fact that the polymer comprises two or more separately produced components. It is believed that the multimodal nature of the claimed composition allows improvements in processing properties. It is preferred therefore if there is multimodality in the ethylene content of the components.
- This can be achieved using a homopolymer and copolymer composition but where both components of the polymer are copolymeric, it is required that the polymers are different to ensure that the polymer composition is multimodal. Preferably therefore, where both components are copolymeric the nature of the comonomer used in each component will be different or the amount of comonomer used in each component will be different, e.g. at least differing by 1 wt%, e.g. at least 2 wt%, preferably at least 3 wt%.
- Since the composition is multimodal, the molecular weight distribution of the composition is an important factor.
- Such multimodal polymers may be prepared by simple blending, by two or more stage polymerisation or by the use of two or more different polymerisation catalysts in a one stage polymerisation. Preferably however they are produced in a two-stage polymerisation using the same catalyst, e.g. a metallocene catalyst or preferably a Ziegler-Natta catalyst, in particular a slurry polymerisation in a loop reactor followed by a gas phase polymerisation in a gas phase reactor.
Conventional cocatalysts, supports/carriers, electron donors etc. can be used. - A loop reactor - gas phase reactor system is marketed by Borealis A/S, Denmark as a BORSTAR reactor system. The polymer of the invention is thus preferably formed in a two stage process comprising a first slurry loop polymerisation followed by gas phase polymerisation in the presence of a Ziegler-Natta catalyst.
- The conditions used in such a process are well known. For slurry reactors, the reaction temperature will generally be in the
range 60 to 110°C (e.g. 85-110°C), the reactor pressure will generally be in therange 5 to 80 bar (e.g. 50-65 bar), and the residence time will generally be in the range 0.3 to 5 hours (e.g. 0.5 to 2 hours). The diluent used will generally be an aliphatic hydrocarbon having a boiling point in the range -70 to +100°C. In such reactors, polymerisation may if desired be effected under supercritical conditions. - For gas phase reactors, the reaction temperature used will generally be in the
range 60 to 115°C (e.g. 70 to 110°C), the reactor pressure will generally be in therange 10 to 25 bar, and the residence time will generally be 1 to 8 hours. The gas used will commonly be a non-reactive gas such as nitrogen or low boiling point hydrocarbons such as propane together with the monomer (i.e. propylene and ethylene when required). - Preferably, component A of the polymer of the invention is produced in a continuously operating loop reactor where propylene (and comonomer when required) are polymerised in the presence of a polymerisation catalyst as stated above and a chain transfer agent such as hydrogen. The diluent is typically an inert aliphatic hydrocarbon, preferably isobutane or propane.
- Component B can then be formed in a gas phase reactor using the same catalyst. Prepolymerisation can be employed as is well known in the art. Ziegler-Natta catalysts are preferred. The nature of the Ziegler-Natta catalyst is described in numerous prior publications, e.g.
US 5234879 . - Alternatively, the polymers of the invention can be made by blending two random copolymers of propylene or by blending one random copolymer with a polypropylene homopolymer in a conventional blending apparatus.
- Random copolymers of propylene and propylene homopolymers of use in this invention are commercially available from various suppliers, e.g. Borealis A/S.
- The polymer composition of the present invention has a higher MFR than those known in the art. In order to achieve sufficiently high MFR values it may be necessary to modify the propylene polymers and copolymers. Propylene polymers and copolymers can be modified by chemical cracking of the polymer chains often called visbreaking. Visbreaking is carried out in an extruder before moulding operations using organic peroxides with relatively high molar mass in a controlled manner. Statistically higher molar mass chains are cleaved more frequently than are lower molar mass molecules, resulting in an overall decrease in the average molar mass and an increase in MFR. The amount of peroxide fed into the extruder is controlled to reach the desired molar mass and MFR, and depends on the MFR of the reactor product. The formed polypropylene is often termed controlled rheology polypropylene and shows a number of advantages regarding processability, mechanics and optics.
- Suitable amounts of peroxide are around 0.01 to 0.1 1 wt%.
- The polymer composition of the invention can include minor amounts of standard polymer additives such as polymer processing agent, nucleating agents, anti-oxidants, UV stabilisers etc.
- The polymers of the invention are suitable for use in the manufacture of films or articles by injection moulding, film blowing, film casting or by blow moulding. In particular, the polymers of the invention are suitable for the production of articles having biaxial molecular orientation manufactured using ISBM processes.
- Preferred articles are bottles, e.g. of 100 ml to 10 L in volume, e.g. 300 ml or 500 ml.
- Biaxial orientation improves the physical and optical properties of the polymer, as well as improving the barrier properties. Biaxial molecular orientation is achieved by stretching the polymer at temperatures below the polymer melting point. In ISBM processes biaxial stretching is achieved in the stretch blow moulding step.
- Two types of ISBM process are practised. In the single-stage process a preform is injection moulded and blown before it is allowed to cool. In the two-stage process the injection moulded preform is allowed to cool before it is reheated and blown into a container. These processes are well known and the person skilled in the art would be able to choose appropriate process conditions.
- Ideally however, the stretching temperatures used are between 110°C and 160 °C, e.g. 130°C. Stretching speeds may range from 20 to 40 m/min in both TD and MD.
- Control of the temperature of the polymer during the biaxial stretching step is critical. If the temperature is too high the stretched polymer will include areas of melted polymer, which reduces the molecular orientation, and will show variation in sample thickness. If the temperature is too low it will not be possible to biaxially stretch the polymer without the polymer failing. The processing window for any given polymer is the temperature range over which the polymer can in practice be biaxially stretched.
- In the Examples discussed below and for the processing window ranges above, the processing window for biaxial stretching is defined as the difference between the Max. temp and Min. temp wherein:
- Max. temp =
- the temperature at which a driving force of ION is required to stretch the polymer
- Min. temp =
- the lowest temperature at which stretching of the polymer is possible without polymer failure
- The polymer compositions of the invention exhibit excellent mechanical and optical properties. Haze values of less than 10%, preferably less than 8% are achievable. It is envisaged that the polymer composition of the invention, when biaxially stretched results in a surface of more perfect molecular orientation leading to improved clarity.
- Tensile modulus values of greater than 600 MPa, e.g. greater than 650 MPa, preferably greater than 700 MPa are also achievable with the polymer composition of the invention. In general, higher ethylene contents are associated with lower tensile modulus values.
- Charpy (23°C), notched values are of the order of 5 to 10 kJ/m2.
- The invention will now be described further with reference to the following non-limiting examples and Figures. Figure 1 is a plot of the drawing force in the transverse direction as a function of the drawing temperature for Example 1 and Comparative Example 1. Figure 2 show the processing window for each of Examples 1 to 6, and Comparative Examples 1 and 2. Figure 3 shows Haze as a function of drawing temperature for
samples - Values quoted in the description/examples are measured according to the following tests:
- a) Xylene Solubles (XS):
For the determination of the xylene solubles fraction, 2.0 g of polymer is dissolved in 250 ml p-xylene at 135°C under agitation. After 30± 2 min the solution is allowed to cool for 15 min at ambient temperature and then allowed to settle for 30 min at 25 ± 0.5°C. The solution is filtered with filter paper into two 100 ml flasks.
The solution from the first 100 ml vessel is evaporated in nitrogen flow and the residue is dried under vacuum at 90°C until constant weight is reached. The xylene soluble fraction is calculated using the following equation:
wherein- mo = initial polymer amount (g),
- ml = weight of residue (g),
- vo = initial volume (ml),
- vl = volume of analysed sample (ml).
- b) Melt flow rate (MFR)
MFR2 was measured according to ISO 1133 at 230°C and a load of 2.16 kg. - c) Haze was measured according to ASTM D1003 on drawn film of 0.2mm thickness.
- d) Thermal Properties
Melting temperature Tm and the degree of crystallinity were measured with a Mettler TAB20 differential scanning calorimetry (DSC) on 3 ± 0.5 mg samples. Both crystallisation and melting curves were obtained during 10°C/min cooling and heating scans between 30° and 225°C. Melting and crystallisation temperatures were taken as the peaks of endotherms and exotherms. The degree of crystallinity was calculated by comparison with the heat of fusion of perfectly crystalline polypropylene i.e. 209 J/g. - e) Viscosity function and Shear Thinning (SHI)
Dynamic rheological measurements were carried out with Rheometrics RDA-II QC on compression molded samples under nitrogen atmosphere at 200°C using 25 mm diameter plate and plate geometry. The oscillatory shear experiments were done within the linear viscoelastic range of strain at frequencies from 0.01 to 500 rad/s. (ISO6721-1)
The values of storage modulus (G'), loss modulus (G"), complex modulus (G*) and complex viscosity (h*) were obtained as a function of frequency (w).
The Zero shear viscosity (h0) was calculated using complex fluidity defined as the reciprocal of complex viscosity. Its real and imaginary part are thus defined by
and
From the following equations
The polydispercity index, PI, is calculated from cross-over point of G'(w) and G"(w).
There is a linear correlation between f' and f" with zero ordinate value of 1 /h0 (Heino et al.1)
For polypropylene this is valid at low frequencies and five first points (5 points/decade) are used in calculation of h0.
Elasticity indexes (G') and shear thinning indexes (SHI), which are correlating with MWD and are independent of MW, were calculated according toHeino 1, 2).
SHI is calculated by dividing the Zero Shear Viscosity by a complex viscosity value, obtained at a certain constant shear stress value, G*. The abbreviation, SHI (0/50), is the ratio between the zero shear viscosity and the viscosity at the shear stress of 50 000 Pa.- 1) Rheological characterization of polyethylene fractions. Heino, E.L.; Lehtinen, A; Tanner, J.; Seppälä, J. Neste Oy, Porvoo, Finland. Theor. Appl. Rheol., Proc. Int. Congr. Rheol., 11th (1992), 1 360-362
- 2)The influence of molecular structure on some rheological properties of polyethylene. Heino, Eeva-Leena. Borealis Polymers Oy, Porvoo, Finland. Annual Transactions of the Nordic Rheology Society, 1995
- f) Comonomer content was determined by C13NMR.
The C13NMR spectra of polypropylenes were recorded on Bruker 400MHz spectrometer at 130°C from samples dissolved in 1,2,4-trichlorobenzene/benzene-d6 (90/10 w/w). For the pentad analysis the assignment is done according to the methods described in literature.
(T. Hayashi, Y. Inoue, R. Chüjö, and T. Asakura, Polymer 29 138-43 (1988).and Chujo R, et al,Polymer 35 339 (1994).
Meso run length was determined from mmmm and mmmr pentads
MRL= 2 x mmmm/ mmmr. - g) Tensile Modulus and stress at yield are measured according to ISO527-2
- h) Charpy, notched is measured according to ISO 179/1eA at 23°C
- i) Density is measured according to ISO 1183
- k) SEC: The molecular weights and molecular weight distributions of polymers were determined with A Millipore Waters ALC/GPC operating at 135 °C and equipped with two mixed bed and one 107 Å TSK-Gel columns (TOSOHAAS 16S) and a differential refractometer detector. The solvent 1,2,4-trichlorobezene was applied at flow rate of 1 ml/min. The columns were calibrated with narrow molecular weight distribution polystyrene standards and narrow and broad polypropylenes.
- The following polymers were employed in the sample formulations:
- (i) A random copolymer of propylene and ethylene having an ethylene content of 4.2 wt.% and an MFR is 1.5 g/10 min.
- (ii) A polypropylene homopolymer having an MFR of 12.0 g/10 min, a density of 908 kg/m3.
- (iii) A random copolymer of propylene and ethylene having an ethylene content of 1 wt.% and an MFR is 1.5 g/10 min.
- (iv) A random copolymer of propylene and ethylene having a ethylene content of 5.8 wt% and an MFR of 8 g/10min.
- (v) A propylene homopolymer having an MFR of 10 g/10 min
- (vi) A random copolymer of propylene and ethylene having a ethylene content of 3.2 wt% and an MFR of 13 g/10min
- (vii) A random copolymer of propylene and ethylene having a ethylene content of 3.2 wt% and an MFR of 30 g/10min
- (viii) A random copolymer of propylene and ethylene having a ethylene content of 3.3 wt% and an MFR of 20 g/10min.
-
Sample 1 is a 60/40 wt.% blend of polymers (iv) and (v) respectively, prepared by physical mixing of polymers (iv) and (v) for 3 minutes, followed by compounding in a Prism 24mm double screw extruder at the conditions:Set temperature 230°C (melt temperature 250°C) N2 pressure: 1.5 bars Speed: 300 rpm Die Pressure: 80 bars -
Sample 2 is a 65/35 wt.% blend of polymers (i) and (ii) respectively, prepared by physical mixing of polymers (i) and (ii) for 3 minutes, followed by compounding in a Prism 24mm double screw extruder at the conditions forsample 1. - In addition 0.05 wt.% of the peroxide Trigonox 101 was added to the blend before physical mixing.
-
Samples 3 to 5 are formed by blending polymer (i) and (iii) in a 60:40 weight ratio, prepared by physical mixing of polymers (i) and (iii) for 3 minutes, followed by compounding in a Prism 24mm double screw extruder at the conditions forsample 1. - In addition, 0.02 wt.%, 0.04 wt.% and 0.06 wt.% of the peroxide Trigonox 101 were added
Sample 3,Sample 4 andSample 5 respectively, before physical mixing of the blends. -
Sample 6 is formed by blending polymer (i) and (iii) in a 50:50 weight ratio, prepared by physical mixing of polymers (i) and (iii) for 3 minutes, followed by compounding in a Prism 24mm double screw extruder at the conditions forsample 1. - In addition 0.06 wt.% of the peroxide Trigonox 101 was added before physical mixing of the blend.
- A continuous multistage process was used to produce a polymer blend. The process comprised a prepolymerisation step, a loop reactor polymerisation and a fluidized bed gas phase reactor polymerisation.
- The catalyst used was highly active, stereospecific transesterified MgCl2-supported Ziegler-Natta catalyst prepared according to
US 5,234,879 at a titanization temperature of 135 °C. The catalyst was contacted with a cocatalyst (triethylaluminium, TEAL), and an external donor (donor D, dicyclopentyl dimethoxysilane) with the Al/Ti ratio of 200 and an Al/D ratio of 5, to yield the catalyst system. - The catalyst system and propylene were fed into the prepolymerisation reactor which was operated at 30°C. The prepolymerised catalyst was used in the subsequent polymerisation reactors.
- Propylene and hydrogen and the prepolymerised catalyst were fed into the loop reactor which was operated as a bulk reactor at the temperatures as indicated in Table 1 and a pressure of 55 bar.
- Then, the polymer slurry stream was fed from the loop reactor into the gas phase reactor which was operated at the temperatures as indicated in Table 1 and a pressure of 20 bar. Propylene, ethylene and hydrogen were fed into the gas phase reactor to control the desired properties of the final polymer.
Table 1 Unit Example 7 Al/D mol/ mol 5 Al/Ti mol/mol 200 Production split (loop:GPR) mol 42:58 Loop Temperature °C 85 MFR g/10 min 20.9 GPR Temperature °C 85 Final Product Ethylene wt.% 3.7 MFR2 g/10 min 19 XS wt.% 10.3 Tm °C 165 Crystallinity % 35 SHI(0/50) Pa 5.8 - Comparative Example 1 is formed from polymer (vi) only and comparative Example 2 formed from polymer (vii) only.
- Details of the polymers produced and the polymers used in Comparative Examples 1 and 2 are provided in Table 2.
Table 2 MFR g/10min Ethylene content / wt % Composition Sample 1 9 3.5 60/40 polymer (iv) and (v) Sample 230* 2.7 65:35 blend of polymer (i) and (ii) Sample 310* 3 60:40 blend of polymers (i) and (iii) Sample 420* 3 60:40 blend of polymers (i) and (iii) Sample 530* 3 60:40 blend of polymers (i) and (iii) Sample 630* 2.7 50:50 blend of polymers (i) and (iii) Sample 719 3.7 Reactor blend of homopolypropylene and propylene/ethylene random copolymer Comp Ex 1 12 3.2 polymer (vi) Comp Ex 230 3.2 poylmer (vii) *visbroken - The Polymer compositions of
samples 1 to 6 and Comparative Examples 1 and 2 were stretched in a laboratory stretching frame in order to simulate the stretching stage of an ISBM process. - Boxes of 35 cm x 15 cm x 10 cm, with a thickness of 2mm, were injection moulded at Netstal 1570/300 MPS injection moulding machine at 230°C with an injection speed of 100 mm/s, a holding pressure to 315 grams product weight of box and a holding time of 12 s. Dosing at backpressure of 100 bar and 150 rpm. The mould temperature was 30°C on injection side and 15°C on clamping side. The cooling time was 15 s. From the bottom of these boxes samples of about 86mm x 86mm x 2mm were cut for biaxial drawing in a laboratory film stretcher KARO IV (Brückner Maschinenbau GmbH, Siegsdorf, Germany) at VTT, Tampere, Finland. The plaques were heated in a heating chamber by IR radiation, for a defined period of time 120s before drawing. To simulate as much as possible the ISBM process, the maximum stretch speed of 35m/min was used. The stretch ratio of 3.5 x 3.5 was selected in order to achieve a thickness reduction from 2 mm to 0.2mm (same as in ISBM process). During the simultaneous drawing, force elongation curves were recorded in the machine direction and in the transverse direction.
- For each sample the temperature range over which the sample could be stretched without producing visible failures was studied (the processing window).
- Plots of the drawing force in the transverse direction as a function of the drawing temperature for Example 1 and Comparative Example 1 are shown in Figure 1. It can be clearly seen that the polymer of the present invention has a broader process window for biaxial stretching than the random copolymer of the Comparative Example.
- Figure 2 and Table 3 show the processing window for each of Examples 1 to 6, and Comparative Examples 1 and 2. The processing window is represented by the shaded area. The number shown for each Example is the processing window in °C.
Table 3 Polymer Processing window ° C Sample 1 20 Sample 217 Sample 317 Sample 419 Sample 517 Sample 618 Comp 19 Comp 212 - The polymers of the present invention provide a significantly broader processing window for ISBM processes than the polymers of the Comparative Examples.
- Biaxial orientation of polypropylene improves the optical properties of the polymer. In this
investigation 2 mm thick injection moulded plaques, are biaxially drawn with a draw ratio (3.5 x 3.5), resulting in 0.2 mm thick films (as described in Example 1). Haze values have been measured for the films drawn at different temperatures. The polymers of Examples 2, 5 and 6 were compared with a sample of polymer (viii) (Comparative Example 3). The results are presented in Figure 3. - The results show that the clarity of the polymers improves with increasing stretching temperature. At stretching temperatures higher that 150 °C the analysed materials have comparable optical properties. At processing temperatures below 150°C, however, the optical properties of the polymers of the invention are much better than those of Comparative Example 3.
- All the materials were clarified with the same concentration of 1,3:2,4-bis(3,4-dimethylbenzylidene sorbitol.
Claims (11)
- A multimodal polymer composition comprising:(A) a polypropylene homopolymer or a propylene random copolymer comprising propylene and up to 5 weight % of comonomer selected from ethylene and/or C4-10 alpha olefin; and(B) a random copolymer of propylene and comonomer selected from ethylene and/or C4-10 alpha olefin;wherein the total comonomer content of the polymer composition is at least 0.5 wt% and the melt flow rate of the polymer blend is at least 6 g/10 min when measured according to ISO 1133 at 230°C and a load of 2.16 kg.
- A composition as claimed in claim 1 wherein component (A) is a homopolymer.
- A composition as claimed in claim 1 or 2 wherein component (B) is a propylene ethylene copolymer.
- A composition as claimed in any one of claims 1 to 3 wherein ethylene content of the composition is at least 2.5 wt%.
- A composition as claimed in any one of claims 1 to 4 wherein the average no. of chain disruptor units is greater than 50 per 1000 propylene repeating units.
- A composition as claimed in any one of claims 1 to 5 having an MFR of 8 to 30 g/10min.
- A composition as claimed in any one of claims 1 to 6 having a processing window of at least 15°C.
- A process for the preparation of an article, the process comprising injection moulding a polymer composition as hereinbefore defined to prepare a preform and subsequently biaxially stretching and blowing the preform at a temperature below the melting point of the polymer.
- A process for the preparation of a polymer composition as hereinbefore described the comprising in a first slurry stage polymerising propylene and optionally ethylene and/or C4-10 alpha olefin in the presence of a Ziegler Natta catalyst so as to form(A) a polypropylene homopolymer or a propylene random copolymer comprising propylene and up to 5 weight % of comonomer selected from ethylene and/or C4-10 alpha olefin;
transferring the product mixture to a gas phase reactor and subsequently polymerising propylene and ethylene and/or C4-10 alpha olefin so as to form(B) a random copolymer of propylene and comonomer selected from ethylene or C4-10 alpha olefin;
wherein the total comonomer content of the polymer composition is at least 0.5 weight % and the melt flow rate of the polymer blend is at least 6 g/10 min when measured according to ISO 1133 at 230°C and a load of 2.16 kg. - Use of a polymer composition as hereinbefore described for the manufacture of a film or article by blow moulding, film blowing, film casting or ISBM.
- A film or article having biaxial molecular orientation comprising a polymer composition as hereinbefore described.
Priority Applications (8)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
EP05257141A EP1788023A1 (en) | 2005-11-21 | 2005-11-21 | Multimodal polypropylene polymer composition |
EA200801167A EA015383B1 (en) | 2005-11-21 | 2006-11-20 | Multimodal polymer composition, use thereof, article and process for the preparation thereof |
EP06818686A EP1963422B1 (en) | 2005-11-21 | 2006-11-20 | Multimodal polypropylene polymer composition |
US12/085,252 US20090306271A1 (en) | 2005-11-21 | 2006-11-20 | Multimodal Polypropylene Polymer Composition |
CN2006800432687A CN101313026B (en) | 2005-11-21 | 2006-11-20 | Multimodal polypropylene polymer composition |
DE602006017737T DE602006017737D1 (en) | 2005-11-21 | 2006-11-20 | MULTIMODAL POLYPROPYLENE POLYMER COMPOSITION |
AT06818686T ATE485340T1 (en) | 2005-11-21 | 2006-11-20 | MULTIMODAL POLYPROPYLENE POLYMER COMPOSITION |
PCT/EP2006/011121 WO2007057224A1 (en) | 2005-11-21 | 2006-11-20 | Multimodal polypropylene polymer composition |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
EP05257141A EP1788023A1 (en) | 2005-11-21 | 2005-11-21 | Multimodal polypropylene polymer composition |
Publications (1)
Publication Number | Publication Date |
---|---|
EP1788023A1 true EP1788023A1 (en) | 2007-05-23 |
Family
ID=36129820
Family Applications (2)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
EP05257141A Withdrawn EP1788023A1 (en) | 2005-11-21 | 2005-11-21 | Multimodal polypropylene polymer composition |
EP06818686A Active EP1963422B1 (en) | 2005-11-21 | 2006-11-20 | Multimodal polypropylene polymer composition |
Family Applications After (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
EP06818686A Active EP1963422B1 (en) | 2005-11-21 | 2006-11-20 | Multimodal polypropylene polymer composition |
Country Status (7)
Country | Link |
---|---|
US (1) | US20090306271A1 (en) |
EP (2) | EP1788023A1 (en) |
CN (1) | CN101313026B (en) |
AT (1) | ATE485340T1 (en) |
DE (1) | DE602006017737D1 (en) |
EA (1) | EA015383B1 (en) |
WO (1) | WO2007057224A1 (en) |
Cited By (25)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO2008087041A1 (en) * | 2007-01-19 | 2008-07-24 | Borealis Technology Oy | Polypropylene-based resin composition and molded article thereof |
EP2014714A1 (en) * | 2007-07-11 | 2009-01-14 | Borealis Technology Oy | Heterophasic polyolefin composition |
WO2010057916A1 (en) * | 2008-11-21 | 2010-05-27 | Borealis Ag | Method for improving flowability of random polypropylene powder |
US20110132864A1 (en) * | 2007-08-10 | 2011-06-09 | Borealis Technology Oy | Article |
WO2011131639A1 (en) * | 2010-04-21 | 2011-10-27 | Borealis Ag | Propylene/1-hexene copolymer composition with low sealing temperature |
WO2011131637A1 (en) * | 2010-04-21 | 2011-10-27 | Borealis Ag | Propylene/1-hexene copolymer composition with broad sealing window |
WO2012126759A1 (en) | 2011-03-18 | 2012-09-27 | Ineos Manufacturing Belgium Nv | Propylene-ethylene random copolymer |
WO2015091839A1 (en) * | 2013-12-18 | 2015-06-25 | Borealis Ag | Bopp film with improved stiffness/toughness balance |
US9670347B2 (en) | 2013-08-14 | 2017-06-06 | Borealis Ag | Propylene composition with improved impact resistance at low temperature |
US9670293B2 (en) | 2013-10-29 | 2017-06-06 | Borealis Ag | Solid single site catalysts with high polymerisation activity |
US9708481B2 (en) | 2013-10-24 | 2017-07-18 | Borealis Ag | Blow molded article based on bimodal random copolymer |
US9751962B2 (en) | 2013-11-22 | 2017-09-05 | Borealis Ag | Low emission propylene homopolymer with high melt flow |
US9777142B2 (en) | 2013-08-21 | 2017-10-03 | Borealis Ag | High flow polyolefin composition with high stiffness and toughness |
US9802394B2 (en) | 2013-10-11 | 2017-10-31 | Borealis Ag | Machine direction oriented film for labels |
US9828698B2 (en) | 2013-12-04 | 2017-11-28 | Borealis Ag | Phthalate-free PP homopolymers for meltblown fibers |
US9890275B2 (en) | 2013-08-21 | 2018-02-13 | Borealis Ag | High flow polyolefin composition with high stiffness and toughness |
US10030109B2 (en) | 2014-02-14 | 2018-07-24 | Borealis Ag | Polypropylene composite |
US10040930B2 (en) | 2013-09-27 | 2018-08-07 | Abu Dhabi Polymers Co. Ltd (Borouge) Llc. | Polymer composition with high XS, high Tm suitable for BOPP processing |
US10100185B2 (en) | 2014-02-06 | 2018-10-16 | Borealis Ag | Soft copolymers with high impact strength |
US10100186B2 (en) | 2014-02-06 | 2018-10-16 | Borealis Ag | Soft and transparent impact copolymers |
US10227427B2 (en) | 2014-01-17 | 2019-03-12 | Borealis Ag | Process for preparing propylene/1-butene copolymers |
WO2019197383A1 (en) * | 2018-04-10 | 2019-10-17 | Borealis Ag | Bimodal polypropylene random copolymer with improved gamma-irradiation resistance |
US10450451B2 (en) | 2014-05-20 | 2019-10-22 | Borealis Ag | Polypropylene composition for automotive interior applications |
US10519259B2 (en) | 2013-10-24 | 2019-12-31 | Borealis Ag | Low melting PP homopolymer with high content of regioerrors and high molecular weight |
WO2021058533A1 (en) * | 2019-09-24 | 2021-04-01 | Sabic Global Technologies B.V. | Biaxially oriented pipe |
Families Citing this family (11)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
EP2223943B1 (en) * | 2009-02-25 | 2011-10-19 | Borealis AG | Multimodal polymer of propylene, composition containing the same and a process for manufacturing the same |
EP2386604B1 (en) * | 2010-04-20 | 2018-11-28 | Borealis AG | Polypropylene bottles |
ES2527333T5 (en) * | 2011-02-14 | 2021-08-02 | Borealis Ag | Sealant Propylene Copolymer |
BR112015006121B1 (en) * | 2012-09-19 | 2021-04-27 | Ineos Europe Ag | COMPOSITION OF RANDOMIZED PROPYLENE-ETHYLENE COPOLYMER, ARTICLE MOLDED BY INJECTION UNDERSTANDING THE SUCH COMPOSITION AND PROCESS FOR THE PRODUCTION OF THE SAME |
CN104812779B (en) * | 2012-12-03 | 2017-08-25 | 埃克森美孚化学专利公司 | Acrylic polymers |
EP2886600B1 (en) | 2013-12-19 | 2018-05-30 | Abu Dhabi Polymers Co. Ltd (Borouge) LLC. | Multimodal polypropylene with respect to comonomer content |
EP3209714A1 (en) * | 2014-10-22 | 2017-08-30 | SABIC Global Technologies B.V. | Thinwall moldable coductive compositions with improved physical properties and uses thereof |
EP3608364A1 (en) * | 2018-08-06 | 2020-02-12 | Borealis AG | Multimodal propylene random copolymer based composition suitable as hot melt adhesive composition |
CN112912436B (en) * | 2018-10-30 | 2023-07-07 | 北欧化工公司 | Polymer compositions suitable for gamma ray sterilization |
WO2020099564A1 (en) * | 2018-11-15 | 2020-05-22 | Abu Dhabi Polymers Co. Ltd (Borouge) L.L.C. | Polymer composition for blow molding applications |
CN113227173B (en) * | 2018-11-15 | 2023-04-28 | 博里利斯股份公司 | Propylene-butene copolymers |
Citations (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
EP0339804A2 (en) * | 1988-04-29 | 1989-11-02 | Exxon Chemical Patents Inc. | Modified polypropylene, process for making article made from the same |
WO1998010016A1 (en) * | 1996-09-04 | 1998-03-12 | Exxon Chemical Patents Inc. | Improved propylene polymers for oriented films |
EP1170305A1 (en) * | 2000-07-05 | 2002-01-09 | ATOFINA Research | Production of polyolefins having improved properties |
WO2002070572A2 (en) * | 2001-03-06 | 2002-09-12 | Exxonmobil Chemical Patents Inc. | Propylene polymers for films |
US20030162907A1 (en) * | 2000-12-22 | 2003-08-28 | Anteo Pelliconi | Polyolefin sheets for thermoforming |
Family Cites Families (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
GB2322376B (en) | 1997-02-25 | 2000-11-29 | Solvay | Polypropylene block copolymers and containers made therefrom |
US7303795B2 (en) * | 2003-03-13 | 2007-12-04 | Invista North America S.A. R.L. | Molding of polypropylene with enhanced reheat characteristics |
DE602005012398D1 (en) | 2004-08-18 | 2009-03-05 | Basell Poliolefine Srl | STRETCH-BLOWED CONTAINERS OF ZIEGLER-NATTA-PROPYLENE POLYMER COMPOSITIONS |
PL1724303T3 (en) * | 2005-05-20 | 2010-03-31 | Borealis Tech Oy | Polypropylene of improved processability for production of pipes |
-
2005
- 2005-11-21 EP EP05257141A patent/EP1788023A1/en not_active Withdrawn
-
2006
- 2006-11-20 EP EP06818686A patent/EP1963422B1/en active Active
- 2006-11-20 DE DE602006017737T patent/DE602006017737D1/en active Active
- 2006-11-20 US US12/085,252 patent/US20090306271A1/en not_active Abandoned
- 2006-11-20 AT AT06818686T patent/ATE485340T1/en not_active IP Right Cessation
- 2006-11-20 CN CN2006800432687A patent/CN101313026B/en active Active
- 2006-11-20 EA EA200801167A patent/EA015383B1/en not_active IP Right Cessation
- 2006-11-20 WO PCT/EP2006/011121 patent/WO2007057224A1/en active Application Filing
Patent Citations (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
EP0339804A2 (en) * | 1988-04-29 | 1989-11-02 | Exxon Chemical Patents Inc. | Modified polypropylene, process for making article made from the same |
WO1998010016A1 (en) * | 1996-09-04 | 1998-03-12 | Exxon Chemical Patents Inc. | Improved propylene polymers for oriented films |
EP1170305A1 (en) * | 2000-07-05 | 2002-01-09 | ATOFINA Research | Production of polyolefins having improved properties |
US20030162907A1 (en) * | 2000-12-22 | 2003-08-28 | Anteo Pelliconi | Polyolefin sheets for thermoforming |
WO2002070572A2 (en) * | 2001-03-06 | 2002-09-12 | Exxonmobil Chemical Patents Inc. | Propylene polymers for films |
Cited By (43)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO2008087041A1 (en) * | 2007-01-19 | 2008-07-24 | Borealis Technology Oy | Polypropylene-based resin composition and molded article thereof |
EP2014714A1 (en) * | 2007-07-11 | 2009-01-14 | Borealis Technology Oy | Heterophasic polyolefin composition |
WO2009007132A1 (en) | 2007-07-11 | 2009-01-15 | Borealis Technology Oy | Heterophasic polyolefin composition |
US20110132864A1 (en) * | 2007-08-10 | 2011-06-09 | Borealis Technology Oy | Article |
US9139709B2 (en) * | 2007-08-10 | 2015-09-22 | Borealis Technology Oy | Article |
US8975333B2 (en) | 2008-11-21 | 2015-03-10 | Borealis Ag | Method for improving flowability of random polypropylene powder |
WO2010057916A1 (en) * | 2008-11-21 | 2010-05-27 | Borealis Ag | Method for improving flowability of random polypropylene powder |
KR101444573B1 (en) * | 2010-04-21 | 2014-09-24 | 보레알리스 아게 | Propylene/1-hexene copolymer composition with broad sealing window |
EP2386603A1 (en) * | 2010-04-21 | 2011-11-16 | Borealis AG | Propylene/1-hexene copolymer composition with broad sealing window |
US8779062B2 (en) | 2010-04-21 | 2014-07-15 | Borealis Ag | Propylene/1-hexene copolymer composition with broad sealing window |
WO2011131639A1 (en) * | 2010-04-21 | 2011-10-27 | Borealis Ag | Propylene/1-hexene copolymer composition with low sealing temperature |
RU2530491C2 (en) * | 2010-04-21 | 2014-10-10 | Бореалис Аг | Propylene/1-hexene copolymer composition with broad heat sealing window |
US8889792B2 (en) | 2010-04-21 | 2014-11-18 | Borealis Ag | Propylene/1-hexene copolymer composition with low sealing temperature |
RU2541470C2 (en) * | 2010-04-21 | 2015-02-20 | Бореалис Аг | Composition of copolymer propylene/1-hexene with low temperature of heat sealing |
WO2011131637A1 (en) * | 2010-04-21 | 2011-10-27 | Borealis Ag | Propylene/1-hexene copolymer composition with broad sealing window |
RU2541470C9 (en) * | 2010-04-21 | 2015-04-20 | Бореалис Аг | Composition of copolymer propylene/1-hexene with low temperature of heat sealing |
EP2686382B2 (en) † | 2011-03-18 | 2024-05-15 | INEOS Manufacturing Belgium NV | Propylene-ethylene random copolymer |
WO2012126759A1 (en) | 2011-03-18 | 2012-09-27 | Ineos Manufacturing Belgium Nv | Propylene-ethylene random copolymer |
US9243138B2 (en) | 2011-03-18 | 2016-01-26 | Ineos Manufacturing Belgium Nv | Propylene-ethylene random copolymer |
EP2686382B1 (en) | 2011-03-18 | 2016-08-10 | INEOS Manufacturing Belgium NV | Propylene-ethylene random copolymer |
RU2602894C2 (en) * | 2011-03-18 | 2016-11-20 | Инеос Мэньюфекчуринг Белджиум Нв | Statistic copolymer of propylene with ethylene |
US9670347B2 (en) | 2013-08-14 | 2017-06-06 | Borealis Ag | Propylene composition with improved impact resistance at low temperature |
US9890275B2 (en) | 2013-08-21 | 2018-02-13 | Borealis Ag | High flow polyolefin composition with high stiffness and toughness |
US9777142B2 (en) | 2013-08-21 | 2017-10-03 | Borealis Ag | High flow polyolefin composition with high stiffness and toughness |
US10040930B2 (en) | 2013-09-27 | 2018-08-07 | Abu Dhabi Polymers Co. Ltd (Borouge) Llc. | Polymer composition with high XS, high Tm suitable for BOPP processing |
US9802394B2 (en) | 2013-10-11 | 2017-10-31 | Borealis Ag | Machine direction oriented film for labels |
US9708481B2 (en) | 2013-10-24 | 2017-07-18 | Borealis Ag | Blow molded article based on bimodal random copolymer |
US10519259B2 (en) | 2013-10-24 | 2019-12-31 | Borealis Ag | Low melting PP homopolymer with high content of regioerrors and high molecular weight |
US9670293B2 (en) | 2013-10-29 | 2017-06-06 | Borealis Ag | Solid single site catalysts with high polymerisation activity |
US9751962B2 (en) | 2013-11-22 | 2017-09-05 | Borealis Ag | Low emission propylene homopolymer with high melt flow |
US9828698B2 (en) | 2013-12-04 | 2017-11-28 | Borealis Ag | Phthalate-free PP homopolymers for meltblown fibers |
CN105980457A (en) * | 2013-12-18 | 2016-09-28 | 博里利斯股份公司 | Bopp film with improved stiffness/toughness balance |
WO2015091839A1 (en) * | 2013-12-18 | 2015-06-25 | Borealis Ag | Bopp film with improved stiffness/toughness balance |
US9637602B2 (en) | 2013-12-18 | 2017-05-02 | Borealis Ag | BOPP film with improved stiffness/toughness balance |
CN105980457B (en) * | 2013-12-18 | 2019-03-22 | 博里利斯股份公司 | With improved rigidity/tough sexual balance BOPP film |
US10227427B2 (en) | 2014-01-17 | 2019-03-12 | Borealis Ag | Process for preparing propylene/1-butene copolymers |
US10100185B2 (en) | 2014-02-06 | 2018-10-16 | Borealis Ag | Soft copolymers with high impact strength |
US10100186B2 (en) | 2014-02-06 | 2018-10-16 | Borealis Ag | Soft and transparent impact copolymers |
US10030109B2 (en) | 2014-02-14 | 2018-07-24 | Borealis Ag | Polypropylene composite |
US10450451B2 (en) | 2014-05-20 | 2019-10-22 | Borealis Ag | Polypropylene composition for automotive interior applications |
WO2019197383A1 (en) * | 2018-04-10 | 2019-10-17 | Borealis Ag | Bimodal polypropylene random copolymer with improved gamma-irradiation resistance |
EP4215582A1 (en) * | 2018-04-10 | 2023-07-26 | Borealis AG | Bimodal polypropylene random copolymer with improved gamma-irradiation resistance |
WO2021058533A1 (en) * | 2019-09-24 | 2021-04-01 | Sabic Global Technologies B.V. | Biaxially oriented pipe |
Also Published As
Publication number | Publication date |
---|---|
WO2007057224A1 (en) | 2007-05-24 |
EP1963422A1 (en) | 2008-09-03 |
EA200801167A1 (en) | 2008-12-30 |
CN101313026A (en) | 2008-11-26 |
EP1963422B1 (en) | 2010-10-20 |
US20090306271A1 (en) | 2009-12-10 |
ATE485340T1 (en) | 2010-11-15 |
CN101313026B (en) | 2011-12-14 |
DE602006017737D1 (en) | 2010-12-02 |
EA015383B1 (en) | 2011-08-30 |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
EP1788023A1 (en) | Multimodal polypropylene polymer composition | |
EP2516125B1 (en) | Heterophasic polypropylene with improved balance between stiffness and transparency | |
EP1849827B1 (en) | Propylene polymer composition and oriented film made therefrom | |
EP2449026B1 (en) | High Flow Polypropylene Composition | |
KR101798500B1 (en) | Propylene homopolymer having high melt strength and preparation method thereof | |
RU2526260C2 (en) | Polypropylene bottles | |
US7470756B2 (en) | Propylene random copolymer and process for the production thereof | |
RU2696643C2 (en) | Linear low density polyethylenes, containing a polyolefin composition with an impact resistance modifier | |
KR101441018B1 (en) | Polypropylene composition comprising a propylene homopolymer component | |
EP1778780B1 (en) | Stretch blow-molded containers from ziegler natta propylene polymer compositions | |
US8044135B2 (en) | Polypropylene impact copolymer compositions | |
EP1923200A1 (en) | Article | |
JP5923672B2 (en) | Extrusion blow molding bottle | |
KR20080087082A (en) | Polypropylene composition comprising a propylene copolymer component | |
EP2338657A1 (en) | Heterophasic polypropylene with improved balance between stiffness and transparency | |
US20090171030A1 (en) | Polypropylene-based copolymer and film comprising the polypropylene-based copolymer | |
CN104245821B (en) | Soft bottle | |
KR101842788B1 (en) | Polypropylene resine material for blow molding with high softness and transparency and preparing method same | |
CN116670228A (en) | Polyolefin composition with high transparency | |
JP2000186175A (en) | Propylene-based polymer or polymer composition for biaxially oriented blow molding and vessel | |
CN114423817A (en) | Heterophasic propylene polymer composition with improved performance characteristics | |
US20100144974A1 (en) | Polypropylene-based copolymer and film comprising the polypropylene-based copolymer |
Legal Events
Date | Code | Title | Description |
---|---|---|---|
PUAI | Public reference made under article 153(3) epc to a published international application that has entered the european phase |
Free format text: ORIGINAL CODE: 0009012 |
|
AK | Designated contracting states |
Kind code of ref document: A1 Designated state(s): AT BE BG CH CY CZ DE DK EE ES FI FR GB GR HU IE IS IT LI LT LU LV MC NL PL PT RO SE SI SK TR |
|
AX | Request for extension of the european patent |
Extension state: AL BA HR MK YU |
|
AKX | Designation fees paid | ||
REG | Reference to a national code |
Ref country code: DE Ref legal event code: 8566 |
|
STAA | Information on the status of an ep patent application or granted ep patent |
Free format text: STATUS: THE APPLICATION IS DEEMED TO BE WITHDRAWN |
|
18D | Application deemed to be withdrawn |
Effective date: 20071124 |